Canonical Allele Identifier: CA2067543753
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120727119A= , CM000674.2:g.120727119A= GRCh38
NC_000012.11:g.121164922A= , CM000674.1:g.121164922A= GRCh37
NC_000012.10:g.119649305A= NCBI36
NG_007991.1:g.6352A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.140A= MANE Select ENSP00000242592.4:p.Asp47=
ENST00000242592.8:c.140A= ENSP00000242592.4:p.Asp47=
ENST00000411593.2:c.140A= ENSP00000401045.2:p.Asp47=
ENST00000539690.1:n.252A=
NM_000017.3:c.140A= NP_000008.1:p.Asp47=
NM_001302554.1:c.140A= NP_001289483.1:p.Asp47=
NM_000017.4:c.140A= MANE Select NP_000008.1:p.Asp47=
NM_001302554.2:c.140A= NP_001289483.1:p.Asp47=